Canonical Allele Identifier: CA302201

Gene: SCN3B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123634162G>A , CM000673.2:g.123634162G>A	GRCh38
NC_000011.9:g.123504870G>A , CM000673.1:g.123504870G>A	GRCh37
NC_000011.8:g.123010080G>A	NCBI36
NG_016283.1:g.25446C>T , LRG_421:g.25446C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299333.8:c.629C>T MANE Select	ENSP00000299333.3:p.Ala210Val
ENST00000655686.1:n.535C>T
ENST00000657123.1:c.629C>T	ENSP00000499439.1:p.Ala210Val
ENST00000657191.1:c.629C>T	ENSP00000499755.1:p.Ala210Val
ENST00000659826.1:c.378C>T
ENST00000667790.1:c.*610C>T	ENSP00000499234.1:n.*610C>T
ENST00000299333.7:c.629C>T	ENSP00000299333.3:p.Ala210Val
ENST00000392770.6:c.629C>T	ENSP00000376523.2:p.Ala210Val
ENST00000527125.1:n.2984C>T
ENST00000530277.5:c.629C>T	ENSP00000432785.1:p.Ala210Val
NM_001040151.1:c.629C>T	NP_001035241.1:p.Ala210Val
NM_018400.3:c.629C>T , LRG_421t1:c.629C>T	NP_060870.1:p.Ala210Val
XM_011542897.1:c.629C>T	XP_011541199.1:p.Ala210Val
XR_947858.1:n.1036C>T
XM_011542897.2:c.629C>T	XP_011541199.1:p.Ala210Val
NM_001040151.2:c.629C>T MANE Select	NP_001035241.1:p.Ala210Val
NM_018400.4:c.629C>T	NP_060870.1:p.Ala210Val